| First Author | Burger JL | Year | 2016 |
| Journal | Anal Biochem | Volume | 502 |
| Pages | 64-72 | PubMed ID | 27019154 |
| Mgi Jnum | J:262351 | Mgi Id | MGI:6162372 |
| Doi | 10.1016/j.ab.2016.03.006 | Citation | Burger JL, et al. (2016) Direct nuclear magnetic resonance observation of odorant binding to mouse odorant receptor MOR244-3. Anal Biochem 502:64-72 |
| abstractText | Mammals are able to perceive and differentiate a great number of structurally diverse odorants through the odorant's interaction with odorant receptors (ORs), proteins found within the cell membrane of olfactory sensory neurons. The natural gas industry has used human olfactory sensitivity to sulfur compounds (thiols, sulfides, etc.) to increase the safety of fuel gas transport, storage, and use through the odorization of this product. In the United States, mixtures of sulfur compounds are used, but the major constituent of odorant packages is 2-methylpropane-2-thiol, also known as tert-butyl mercaptan. It has been fundamentally challenging to understand olfaction and odorization due to the low affinity of odorous ligands to the ORs and the difficulty in expressing a sufficient number of OR proteins. Here, we directly observed the binding of tert-butyl mercaptan and another odiferous compound, cis-cyclooctene, to mouse OR MOR244-3 on living cells by saturation transfer difference (STD) nuclear magnetic resonance (NMR) spectroscopy. This effort lays the groundwork for resolving molecular mechanisms responsible for ligand binding and resulting signaling, which in turn will lead to a clearer understanding of odorant recognition and competition. |
